Abstract: A shroud (1020) for a mask system includes a retaining portion structured to retain a frame (1040), a pair of upper headgear connectors (1024) each including an elongated arm (1026) and a slot (1027) at the free end of the arm adapted to receive a headgear strap, and a pair of lower headgear connectors (1025) each adapted to attach to a headgear strap. The retaining portion, the upper headgear connectors, and the lower headgear connectors are integrally formed as a one piece structure.

Abstract: This disclosure describes systems, methods, and apparatus for intubation where indicators of a bougie's axial orientation and insertion depth into the trachea are not visible. In particular, a bougie having one or more tactile indicators of axial orientation and/or depth of insertion are disclosed. The tactile indicators can include finger grooves and/or a ridge to name two examples.

Abstract: A float retention arrangement and related methods for a humidification chamber that includes at least one float that operates an inlet valve that controls a flow of water through a water inlet opening of the humidification chamber. A cover of the humidification chamber defines an interior space, at least one gas port and a float retention opening. A component forms at least a portion of a water supply conduit for supplying water from a water source to the water inlet opening. The component is insertable into the float retention opening and is positionable to contact and retain the at least one float in a non-use position. In some configurations, the component can be a water spike.

Abstract: A mask assembly adapted for use with a positive airway pressure device, includes a mask frame, an elbow assembly provided to the frame, a cushion provided to the frame, a forehead support assembly, and a neck to connect the frame to the forehead support assembly, wherein the neck includes a pair of side walls having a streamlined design that is made to look sleek and reduce or minimize obtrusiveness. The pair of side walls may take the form of a single wall or more than two walls. The mask frame may include a recessed port structure including at least one port having access to an interior of the frame which at least in part with the cushion defines a breathing chamber in communication with a nasal passage of the patient in use. The mask frame may also include a channel to receive the cushion. The channel is formed by an outer wall and an inner wall and the channel includes an inner surface having a bead to engage with an outer surface of an edge of the cushion.

Abstract: A tub is configured to contain a supply of water and is configured to be inserted into a chamber of a humidifier. The tub includes a tub base configured to contain the supply of water. The tub also includes a tub lid and a flow plate provided between the tub base and the tub lid. The flow plate includes a water level indicator configured to indicate a level of the supply of water in the tub base. In addition, the water level indicator includes a generally rectangular portion and a generally triangular portion.

Abstract: A flow generator includes a blower, a flow generator outlet configured to receive an end of a gas delivery tube, and a controller. The flow generator outlet includes electrical connectors configured to contact corresponding electrical connectors associated with the breathable gas delivery tube when the breathable gas delivery tube is received by the flow generator outlet. The controller includes a tube-type detect circuit and is configured to receive signals from the breathable gas delivery tube by way of the electrical connectors of the flow generator outlet. The tube-type detect circuit is configured so that when the breathable gas delivery tube is received by the flow generator outlet, the tube-type detect circuit determines the type of breathable gas delivery tube based on signals from the electrical connectors of the flow generator outlet that are indicative of a condition of a resistor associated with the breathable gas delivery tube.

Abstract: The present disclosure relates to a dose indicator for a pressure-actuated metered dose inhaler (pMDI) device. In an embodiment, the dose indicator comprises a chassis element having a viewing portion, a display element located within the chassis element, a resilient deformable element, and an indexing element having an axis, translation of the indexing element along its axis from a first position to a second position causing deformation of the resilient deformable element in the same direction as translation of the indexing element resulting in generally greater displacement of portions of the resilient deformable element nearer to the axis relative to portions thereof further from the axis, the displacement of the portions of the resilient deformable element in the same direction as translation of the indexing element inducing indexing of the display element from a current position to a subsequent position relative to the viewing portion of the chassis element.

Abstract: A cushion pad for a mask worn by a patient, comprising a first side to contact skin of the patient, and a second side, opposite the first side, to contact or face the mask. The pad has a main body portion having a central portion shaped to cover a portion of the patient's nose extending from above the nose tip to the nasal bridge region without obstructing the patient's line of sight, and lateral side portions to extend downward and terminate along the sides of the nose or on the patient's cheeks. The main body is made of a breathable material, e.g., foam. The pad may include adhesive and/or an attached portion, e.g., a ring, to couple the pad to the patient and/or portion of the mask.

Abstract: The present disclosure relates to absorbent articles and methods for assembling absorbent articles with substrates and/or components that include graphics with zones of relatively high print densities and zones of relatively low print densities. In turn, the zones of relatively low print densities may be positioned in regions that are subject to various manufacturing transformations during the assembly process. As such, the graphics may be positioned and/or printed in such a manner so as to reduce noticeable visible results of imprecise and/or inconsistent manufacturing operations performed in areas where the graphics are located.

Abstract: A cover for a vape pen has a cylindrical body having a closed and an open end, a length substantially shorter than a vape pen to be covered, an outside diameter, and an inside diameter greater than an outside diameter and dimensions of a mouthpiece of the vape pen to be covered, a pocket clip affixed to the outside diameter, aligned in a direction of the length of the cylindrical body, and directed such that in use the closed end of the cylindrical body is uppermost, and an insert affixed to the inside diameter of the cylindrical body, around a circumference of the inside diameter, the insert presenting a plurality of flexible protuberances each of a length less than a radius of the cylindrical body, with each directed radially inward from the inside diameter of the cylindrical body.

Abstract: A nasal cannula according to an embodiment of the present invention includes: an oxygen supplying portion which forms a space inside in which a nose and a mouth of a user can be disposed and is able to supply oxygen in a state of being put on by the user into the nose of the user; and a mask portion to which the oxygen supplying portion is attached in a detachable manner therein and is configured to be put on a face of the user. Since a space in which a nose and a mouth of a user can be disposed is provided inside the oxygen supplying portion so that a user can put on the nasal cannula in a convenient state and the oxygen supplying portion is put on in a state of being supported by the mask portion, oxygen can be supplied into the nose of the user and at the same time external air can be filtered.

Abstract: An air delivery system for providing a supply of air from a source of air at positive pressure to an interfacing structure located at the entrance to the airways of a patient includes a manifold adapted to connect with the supply of positive air pressure and at least one tube connected to the manifold and adapted to deliver the supply of air to the interfacing structure. Each tube is structured to allow movement between an open phase in which the tube allows the passage of air and a collapsed phase in which the tube is collapsed. Each tube is structured such that weight of a typical patient's head against bedding apparel is sufficient to collapse the tube from the open phase to the collapsed phase.

Abstract: A vapor generating system includes a mouthpiece housing including an air outlet at a first side of the mouthpiece housing. The vapor generating system further includes a liquid storage portion, a filamentary wick extending into the liquid storage portion, a heating coil at least partially surrounding a portion of the filamentary wick and a chamber between the heating coil and the air outlet.

Abstract: An inhalation device comprising a housing, a sensor, a microcontroller, and an actuating device controlled by the microcontroller; the housing comprises a mouthpiece having an opening connected to a passage in said housing, wherein the other end of the passage provides an opening for a cartridge; said sensor being in communication with the microprocessor and configured to detect a parameter based on an action to the mouthpiece, and wherein a parameter being reached, the microcontroller engages the actuating device which engages the cartridge to deliver medication through the passage and out of the mouthpiece.

Abstract: Sensing airflow and delivering therapeutic gas to a patient. At least some of the example embodiments are methods including: titrating a patient with therapeutic gas during a period of time when a flow state of breathing orifices is in a first state, the titrating results in a prescription titration volume; and then delivering the prescription titration volume of therapeutic gas to the patient when the flow state of the breathing orifices is in a second state different than the first state, the delivering only to the breathing orifices open to flow.

Abstract: A pulmonary secretion clearing airway structure and related airway management system is disclosed that has a double lumen portion which each lumen of the double lumen portion operably secured to an airway management system so that inspiratory fluid (air/oxygen mixtures, with or without added water vapor) is delivered to the distal end of the ventilation catheter through one of the two lumens and expired inspiratory fluid, pulmonary secretions, and pulmonary fluids are removed from the patient through the other lumen. The expiratory fluid pathway preferably includes a secretion collection system for removing the pulmonary secretions and the like from the pathway, thereby improving operation and safety of the system. The airway structure can be a ventilation catheter or a supraglottic airway system such as laryngeal mask and the like.

Abstract: The systems and methods provide for novel a triggering mode that allows the patient to trigger or initiate the delivery of a breath during ventilation on a ventilator. Further, the systems and methods provide for triggering ventilation utilizing a statistical trigger mode. Additionally, the systems and methods provide for analyzing and/or displaying information related to a potential change in a triggering threshold for a currently utilized breath type.

Abstract: A respiratory component measurement system that includes an airway adapter adapted to be placed in fluid communication with an airway of a patient and a sensor element in physical communication with the airway adapter. The sensor element is adapted to detect an orientation related characteristic of the airway adapter, a motion related characteristic of the airway adapter, or both. A respiratory component sensor is also adapted to be disposed on the airway adapter so as to measure a characteristic associated with a flow of gas through the airway adapter.

Abstract: The present invention discloses a carbon dioxide inhalation treatment device for central sleep apnea comprising a blower, a gas cylinder filled with carbon dioxide (CO2), an airbag, a mask, and a detection mechanism for detecting the central apnea by measuring the electromyographic activity of the chest wall muscles. The mask is provided with multiple holes providing a communication between the inside and outside of the mask in order to prevent any sense of resistance of breathing and to provide greater control of inspired CO2. Inspired CO2 from a gas mixture containing also a minimum 20% O2 is driven by air using a blower into a mixing chamber. This carbon dioxide inhalation treatment device for central sleep apnea can provide a stable, mild level of carbon dioxide for patients with central sleep apnea, thus by preserving respiratory drive correcting central sleep apnea without increasing the arousal and microarousal frequency.

Abstract: The present invention provides a method and apparatus for controlling a patient's body temperature and in particular for inducing therapeutic hypothermia. Various embodiments of the system are described. The system includes: a source of breathing gas, which may be in the form of a compressed breathing gas mixture; a heat exchanger or other heating and/or cooling device; and a breathing interface, such as a breathing mask or tracheal tube. Optionally, the system may include additional features, such as a mechanical respirator, a nebulizer for introducing medication into the breathing gas, a body temperature probe and a feedback controller. The system can use air or a specialized breathing gas mixture, such as He/O2 or SF/O2 to increase the heat transfer rate. In addition, the system may include an ice particle generator for introducing fine ice particles into the flow of breathing gas to further increase the heat transfer rate.